Novel synthetic molecules boost immune response to HIV and prostate cancer

Washington, Nov 6 (ANI): Synthetic molecules developed by researchers at Yale University could enhance the body’s immune response to HIV and HIV-infected cells, and prostate cancer cells.

The findings by Yale researchers could lead to novel therapeutic approaches for these diseases.

The molecules – called “antibody-recruiting molecule targeting HIV” (ARM-H) and “antibody-recruiting molecule targeting prostate cancer” (ARM-P) – work by binding simultaneously to an antibody already present in the bloodstream and to proteins on HIV, HIV-infected cells or cancer cells.

By coating these pathogens in antibodies, the molecules flag them as a threat and trigger the body’s own immune response.

ARM-H molecules also bind to proteins on the outside of the virus and thus prevent healthy human cells from being infected.

“Instead of trying to kill the pathogens directly, these molecules manipulate our immune system to do something it wouldn’t ordinarily do,” said Dr. David Spiegel, the corresponding author of the study.

In contrast to other treatment options for HIV and cancer, the ARM-H and ARM-P molecules, which the team has begun testing in mice, are structurally simple, inexpensive to produce, and could in theory be taken in pill form, said Spiegel.

And because they are unlikely to target essential biological processes in the body, the side effects could be smaller, he said.

“This is an entirely new approach to treating these two diseases, which are extraordinarily important in terms of their impact on human health,” said Spiegel.

The study has been published online in the Journal of the American Chemical Society. (ANI)

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One Response to Novel synthetic molecules boost immune response to HIV and prostate cancer
  1. debbie foster
    December 27, 2009 | 11:49 pm

    I need to know more about these synthetic molecules………could you please give me some information on when and where these clinical trials will begin…….my husband is out of options…………

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